US20070187639A1 - Refrigerant additive compositions containing perfluoropolethers - Google Patents

Refrigerant additive compositions containing perfluoropolethers Download PDF

Info

Publication number
US20070187639A1
US20070187639A1 US11/653,125 US65312507A US2007187639A1 US 20070187639 A1 US20070187639 A1 US 20070187639A1 US 65312507 A US65312507 A US 65312507A US 2007187639 A1 US2007187639 A1 US 2007187639A1
Authority
US
United States
Prior art keywords
butene
trifluoromethyl
propene
pentene
perfluoropolyether
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/653,125
Other languages
English (en)
Inventor
Thomas Leck
Thomas Saturno
Gregory Bell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US11/653,125 priority Critical patent/US20070187639A1/en
Assigned to E. I. DU PONT DE NEMOURS AND COMPANY reassignment E. I. DU PONT DE NEMOURS AND COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BELL, GREGORY A., SATURNO, THOMAS FRANK, LECK, THOMAS J.
Priority to US11/827,256 priority patent/US7759532B2/en
Priority to US11/827,255 priority patent/US8188323B2/en
Publication of US20070187639A1 publication Critical patent/US20070187639A1/en
Priority to US12/796,696 priority patent/US8049046B2/en
Priority to US13/241,540 priority patent/US8426657B2/en
Priority to US13/833,524 priority patent/US8758641B2/en
Priority to US14/277,489 priority patent/US9315709B2/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/04Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa
    • C09K5/041Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems
    • C09K5/044Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds
    • C09K5/045Materials undergoing a change of physical state when used the change of state being from liquid to vapour or vice versa for compression-type refrigeration systems comprising halogenated compounds containing only fluorine as halogen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M171/00Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
    • C10M171/008Lubricant compositions compatible with refrigerants
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2205/00Aspects relating to compounds used in compression type refrigeration systems
    • C09K2205/10Components
    • C09K2205/106Carbon dioxide
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2205/00Aspects relating to compounds used in compression type refrigeration systems
    • C09K2205/10Components
    • C09K2205/12Hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2205/00Aspects relating to compounds used in compression type refrigeration systems
    • C09K2205/10Components
    • C09K2205/12Hydrocarbons
    • C09K2205/126Unsaturated fluorinated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/06Well-defined aromatic compounds
    • C10M2203/065Well-defined aromatic compounds used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/1006Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
    • C10M2205/0285Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • C10M2207/2835Esters of polyhydroxy compounds used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/32Esters of carbonic acid
    • C10M2207/325Esters of carbonic acid used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical
    • C10M2209/043Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/1033Polyethers, i.e. containing di- or higher polyoxyalkylene groups used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2213/00Organic macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2213/06Perfluoro polymers
    • C10M2213/0606Perfluoro polymers used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2221/00Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2221/04Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2221/0405Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/09Characteristics associated with water
    • C10N2020/097Refrigerants
    • C10N2020/099Containing Chlorofluorocarbons
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/09Characteristics associated with water
    • C10N2020/097Refrigerants
    • C10N2020/101Containing Hydrofluorocarbons
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/09Characteristics associated with water
    • C10N2020/097Refrigerants
    • C10N2020/103Containing Hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/09Characteristics associated with water
    • C10N2020/097Refrigerants
    • C10N2020/105Containing Ammonia
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/09Characteristics associated with water
    • C10N2020/097Refrigerants
    • C10N2020/106Containing Carbon dioxide
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/56Boundary lubrication or thin film lubrication
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/30Refrigerators lubricants or compressors lubricants
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency

Definitions

  • the present invention relates to compositions and processes for use in heat transfer, refrigeration and air-conditioning systems to improve the oil return, lubrication, energy efficiency, or reduce compressor wear, by using perfluoropolyether as an additive in the refrigerant or heat transfer fluid composition.
  • Lubricants have been used with the fluids in the heat transfer, refrigeration and air-conditioning systems to provide lubrication to the compressor and other moving parts and reduce compressor wear.
  • refrigerants or heat transfer fluids are compatible with all the lubricants.
  • many HFC refrigerants or heat transfer fluids have poor miscibility or poor dispersibility with commonly used lubricants, such as mineral oil and alkylbenzene.
  • the heat transfer fluids can not readily transport mineral oil lubricants through the heat exchangers, the lubricant oils accumulate on the surface of the heat exchange coils, resulting in poor oil return, poor heat exchange, low energy efficiency and the accelerated wear and tear of the compressors.
  • the refrigeration and air conditioning industries have had to resort to the use of more expensive and more difficult to use synthetic lubricants such as polyolesters and polyalkylene glycols.
  • the present invention relates to a composition including: (1) a refrigerant or heat transfer fluid selected from the group consisting of saturated fluorocarbons, unsaturated fluorocarbons, hydrochlorofluorocarbons, fluoroethers, hydrocarbons, carbon dioxide, dimethyl ether, ammonia and combinations thereof, and (2) perfluoropolyether.
  • This invention further relates to a composition comprising: (1) mineral oil, and (2) perfluoropolyether.
  • This invention further relates to methods of using the refrigeration or heat transfer fluid compositions of the present invention for producing refrigeration or heating.
  • This invention further relates to processes for the transfer of heat from a heat source to a heat sink wherein the compositions of the present invention serve as heat transfer fluids.
  • This invention further relates to processes of using the perfluoropolyether to maintain or improve the oil return, lubrication, or energy efficiency of the refrigeration, air conditioning and heat transfer system.
  • the refrigerants or heat transfer fluids of used in the present invention are selected from the group consisting of saturated fluorocarbons, unsaturated fluorocarbons, chlorofluorocarbons, hydrochlorofluorocarbons, fluoroethers, hydrocarbons, carbon dioxide, dimethyl ether, ammonia and combinations thereof.
  • Preferred refrigerants or heat transfer fluids include saturated and unsaturated fluorocarbons and hydrofluorocarbons.
  • Representative saturated fluorocarbon refrigerants or heat transfer fluids include tetrafluoromethane (PFC-14), hexafluoroethane (PFC-116), octafluoropropane (PFC-218), decafluorobutane (PFC-31-10), fluoromethane (HFC-41), difluoromethane (HFC-32), trifluoromethane (HFC-23), fluoroethane (HFC-161), 1,1-difluoroethane (HFC-152a), 1,1,1-trifluoroethane (HFC-143a), 1,1,1,2-tetrafluoroethane (HFC-134a), 1,1,2,2-tetrafluoroethane (HFC-134), 1,1,1,2,2-pentafluoroethane (HFC-125), 1,1,1,3,3,3-hexafluoropropane (HFC-236fa), 1,1,1,2,3,3,3-hept
  • R410A a blend of 50 wt. % of HFC-32 and 50 wt. % of HFC-125
  • R417A a blend of 46.6 wt. % of HFC-125, 50 wt. % of HFC-134a and 3.4 wt. % of n-butane
  • R-422A a blend of 85.1 wt. % of HFC-125, 11.5 wt. % of HFC-134a, and 3.4 wt. % of isobutane
  • R-407C a blend of 23 wt.
  • HFC-32 25 wt. % of HFC-125 and 52 wt. % of HFC-134a
  • R-507A a blend of 50% R-125 and 50% R-143a
  • R-508A a blend of 39% HFC-23 and 61% PFC-116
  • Representative unsaturated fluorocarbon refrigerants or heat transfer fluids include 1,2,3,3,3-pentafluoro-1-propene, 1,1,3,3,3-pentafluoro-1-propene, 1,1,2,3,3-pentafluoro-1-propene, 1,2,3,3-tetrafluoro-1-propene, 2,3,3,3-tetrafluoro-1-propene, 1,3,3,3-tetrafluoro-1-propene, 1,1,2,3-tetrafluoro-1-propene, 1,1,3,3-tetrafluoro-1-propene, 1,2,3,3-tetrafluoro-1-propene, 2,3,3-trifluoro-1-propene, 3,3,3-trifluoro-1-propene, 1,1,2-trifluoro-1-propene, 1,1,3-trifluoro-1-propene, 1,2,3-trifluoro-1-propene, 1,3,3-trifluoro-1-prop
  • chlorofluorocarbon refrigerants or heat transfer fluids include trichlorofluoromethane (CFC-11), dichlorodifluoromethane (CFC-12), 1,1,1-trichlorotrifluoroethane (CFC-113a), 1,1,2-trichlorotrifluoroethane (CFC-113), and chloropentafluoroethane (CFC-115).
  • hydrochlorofluorocarbon refrigerants or heat transfer fluids include chlorodifluoromethane (HCFC-22), 2-chloro-1,1,1-trifluoroethane (HCFC-123), 2-chloro-1,1,1,2-tetrafluoroethane (HCFC-124) and 1-chloro-1,1-difluoroethane (HCFC-142b).
  • Representative fluoroether refrigerants or heat transfer fluids include CF 3 OCHF 2 , CF 3 OCH 3 , CF 3 OCH 2 F, CHF 2 OCHF 2 , cyclo-(CF 2 CF 2 CF 2 O—), CF 3 CF 2 OCH 3 , CHF 2 OCHFCF 3 , CHF 2 CF 2 OCH 3 , C 4 F 9 OCH 3 , C 4 F 9 OC 2 H 5 , CF 3 OCF 3 , CF 3 OC 2 F 5 , C 2 F 5 OC 2 F 5 and CF 3 OCF(CF 3 )CF(CF 3 )OCF 3 .
  • hydrocarbon refrigerants or heat transfer fluids include methane, ethane, propane, cyclopropane, propylene, n-butane, cyclobutane, 2-methylpropane, methylcyclopropane, n-pentane, cyclopentane, 2-methylbutane, methylcyclobutane, 2,2-dimethylpropane and dimethylcyclopropane isomers.
  • perfluoropolyethers as an additive which is miscible with chlorofluorocarbon and hydrofluorocarbon refrigerants or heat transfer fluids.
  • a common characteristic of perfluoropolyethers is the presence of perfluoroalkyl ether moieties.
  • Perfluoropolyether is synonymous to perfluoropolyalkylether. Other synonymous terms frequently used include “PFPE”, “PFAE”, “PFPE oil”, “PFPE fluid”, and “PFPAE”.
  • KRYTOX available from DuPont is a perfluoropolyether having the formula of CF 3 —(CF 2 ) 2 —O—[CF(CF 3 )—CF 2 —O]j′-R′f. In the formula, j′ is 2-100, inclusive and R′f is CF 2 CF 3 , a C3 to C6 perfluoroalkyl group, or combinations thereof.
  • FOMBLIN-Y can have the formula of CF 3 O(CF 2 CF(CF 3 )—O—) m′ (CF 2 —O—) n′ —R 1f . Also suitable is CF 3 O[CF 2 CF(CF 3 )O] m′ (CF 2 CF 2 O) o′ (CF 2 O) n′ —R 1f .
  • R 1f is CF 3 , C 2 F 5 , C 3 F 7 , or combinations of two or more thereof; (m′+n′) is 8-45, inclusive; and m/n is 20-1000, inclusive; o′ is 1; (m′+n′+o′) is 8-45, inclusive; m′/n′ is 20-1000, inclusive.
  • FOMBLIN-Z can have the formula of CF 3 O(CF 2 CF 2 —O—) p′ (CF 2 —O) q′ CF 3 where (p′+q′) is 40-180 and p′/q′ is 0.5-2, inclusive.
  • DEMNUM fluids another family of PFPE available from Daikin Industries, Japan, can also be used. It can be produced by sequential oligomerization and fluorination of 2,2,3,3-tetrafluorooxetane, yielding the formula of F—[(CF 2 ) 3 —O] t′ —R 2f where R 2f is CF 3 , C 2 F 5 , or combinations thereof and t′ is 2-200, inclusive.
  • the two end groups of the perfluoropolyether can be functionalized or unfunctionalized.
  • the end group can be branched or straight chain perfluoroalkyl radical end groups.
  • Examples of such perfluoropolyethers can have the formula of C r′ F (2r′+1) -A-C r′ F (2r′+1) in which each r′ is independently 3 to 6;
  • A can be 0-(CF(CF 3 )CF 2 —O) w′ , O—(CF 2 —O) x′ (CF 2 CF 2 —O) y′ , O—(C 2 F 4 —O) w′ , O—(C 2 F 4 —O) x′ (C 3 F 6 —O) y′ , O—(CF(CF 3 )CF 2 —O) x′ (CF 2 —O) y′ , O—(CF(CF 3 ) —O) x′ (CF 2 —O) y′ ,
  • halogen atoms include, but are not limited to, F(CF(CF 3 )—CF 2 —O) 9 —CF 2 CF 3 , F(CF(CF 3 )—CF 2 —O) 9 —CF(CF 3 ) 2 , and combinations thereof.
  • up to 30% of the halogen atoms can be halogens other than fluorine, such as, for example, chlorine atoms.
  • the two end groups of the perfluoropolyether can also be functionalized.
  • a typical functionalized end group can be selected from the group consisting of esters, hydroxyls, amines, amides, cyanos, carboxylic acids and sulfonic acids
  • ester end groups include —COOCH 3 , —COOCH 2 CH 3 , —CF 2 COOCH 3 , —CF 2 COOCH 2 CH 3 , —CF 2 CF 2 COOCH 3 , —CF 2 CF 2 COOCH 2 CH 3 , —CF 2 CH 2 COOCH 3 , —CF 2 CF 2 CH 2 COOCH 3 , —CF 2 CH 2 CH 2 COOCH 3 , —CF 2 CH 2 CH 2 COOCH 3 , —CF 2 CF 2 CH 2 CH 2 COOCH 3 .
  • Representative hydroxyl end groups include —CF 2 OH, —CF 2 CF 2 OH, —CF 2 CH 2 OH, —CF 2 CF 2 CH 2 OH, —CF 2 CH 2 CH 2 OH, —CF 2 CF 2 CH 2 CH 2 OH.
  • Representative amine end groups include —CF 2 NR 1 R 2 , —CF 2 CF 2 NR 1 R 2 , —CF 2 CH 2 NR 1 R 2 , —CF 2 CF 2 CH 2 NR 1 R 2 , —CF 2 CH 2 CH 2 NR 1 R 2 , CF 2 CH 2 CH 2 NR 1 R 2 , CF 2 CF 2 CH 2 CH 2 NR 1 R 2 , wherein R 1 and R 2 are independently H, CH 3 , or CH 2 CH 3 .
  • Representative amide end groups include —CF 2 C(O)NR 1 R 2 , —CF 2 CF 2 C(O)NR 1 , R 2 , —CF 2 CH 2 C(O)NR 1 R 2 , —CF 2 CF 2 CH 2 C(O)NR 1 , R 2 , —CF 2 CH 2 CH 2 C(O)NR 1 R 2 , —CF 2 CF 2 CH 2 CH 2 C(O)NR 1 R 2 , wherein R 1 and R 2 are independently H, CH 3 , or CH 2 CH 3 .
  • Representative cyano end groups include —CF 2 CN, —CF 2 CF 2 CN, —CF 2 CH 2 CN, —CF 2 CF 2 CH 2 CN, —CF 2 CH 2 CH 2 CN, —CF 2 CF 2 CH 2 CH 2 CN.
  • Representative carboxylic acid end groups include —CF 2 COOH, —CF 2 CF 2 COOH, —CF 2 CH 2 COOH, —CF 2 CF 2 CH 2 COOH, —CF 2 CH 2 CH 2 COOH, —CF 2 CF 2 CH 2 CH 2 COOH.
  • Representative sulfonic acid end groups include —S(O)(O)OR 3 , S(O)(O)R 4 , —CF 2 O S(O)(O)OR 3 , —CF 2 CF 2 O S(O)(O)OR 3 , —CF 2 CH 2 O S(O)(O)OR 3 , —CF 2 CF 2 CH 2 O S(O)(O)OR 3 , —CF 2 CH 2 CH 2 O S(O)(O)OR 3 , —CF 2 CF 2 CH 2 CH 2 O S(O)(O)OR 3 , —CF 2 S(O)(O)OR 3 , —CF 2 S(O)(O)OR 3 , —CF 2 CF 2 S(O)(O)OR 3 , —CF 2 CH 2 S(O)(O)OR 3 —CF 2 CF 2 CH 2 S(O)(O)OR 3 , —CF 2 CH 2 S(O)(O)OR 3 , —CF
  • the refrigerant-perfluoropolyether additive combination of this invention improves performance of refrigeration, air conditioning and heat transfer system in one or more aspects. In one aspect, it enables adequate oil return to the compressor such that oil levels are maintained at the proper operating level by preventing accumulation of oil in the heat exchanger coils. In another aspect, the refrigerant-perfluoropolyether may also improves lubrication performance of mineral oil and synthetic lubricant oils. In yet another aspect, the refrigerant-perfluoropolyether also improves heat transfer efficiency and thus the energy efficiency. The refrigerant-perfluoropolyether has also been shown to reduce friction and wear in boundary lubrication, which is expected to result in longer compressor life. The advantages listed above are not intended to be exhausting.
  • an effective amount of perfluoropolyether in this application means an amount of perfluoropolyether additive to provide sufficient oil return to the compressor in order to maintain or improve lubrication or energy efficiency performance or both, where said amount of perfluoropolyether is adjusted by one of ordinary skill to a level appropriate to the individual refrigeration/heat transfer system (coil, compressor, etc.) and refrigerant employed.
  • the amount of perfluoropolyether is less than 40% by weight relative to the refrigerant or heat transfer fluid.
  • the amount of perfluoropolyether additive is less than about 20-30 wt. % relative to the refrigerant or heat transfer fluid. More preferably, the perfluoropolyether additive is less than about 10 wt. % relative to the refrigerant or heat transfer fluid. More preferably, the perfluoropolyether additive is less than about 1 to about 2 wt. % relative to the refrigerant or heat transfer fluid. More preferably, the perfluoropolyether additive is between about 0.01 wt. % and 1.0 wt. % relative to the refrigerant or heat transfer fluid. Most preferably, the perfluoropolyether additive is between about 0.03 and 0.80 wt. % relative to the refrigerant or heat transfer fluid.
  • compositions of the present invention may further comprise about 0.01 weight percent to about 5 weight percent of a stabilizer, free radical scavenger or antioxidant.
  • a stabilizer free radical scavenger or antioxidant.
  • Such other additives include but are not limited to, nitromethane, hindered phenols, hydroxylamines, thiols, phosphites, or lactones. Single additives or combinations may be used.
  • refrigeration or air-conditioning system additives may be added, as desired, to compositions of the present invention in order to enhance performance and system stability.
  • additives are known in the field of refrigeration and air-conditioning, and include, but are not limited to, anti wear agents, extreme pressure lubricants, corrosion and oxidation inhibitors, metal surface deactivators, free radical scavengers, and foam control agents.
  • these additives may be present in the inventive compositions in small amounts relative to the overall composition. Typically concentrations of from less than about 0.1 weight percent to as much as about 3 weight percent of each additive are used. These additives are selected on the basis of the individual system requirements.
  • additives include members of the triaryl phosphate family of EP (extreme pressure) lubricity additives, such as butylated triphenyl phosphates (BTPP), or other alkylated triaryl phosphate esters, e.g. Syn-O-Ad 8478 from Akzo Chemicals, tricresyl phosphates and related compounds. Additionally, the metal dialkyl dithiophosphates (e.g. zinc dialkyl dithiophosphate (or ZDDP), Lubrizol 1375 and other members of this family of chemicals may be used in compositions of the present invention.
  • Other antiwear additives include natural product oils and asymmetrical polyhydroxyl lubrication additives, such as Synergol TMS (International Lubricants).
  • stabilizers such as anti oxidants, free radical scavengers, and water scavengers may be employed.
  • Compounds in this category can include, but are not limited to, butylated hydroxy toluene (BHT) and epoxides.
  • Lubricants used in this invention include natural and synthetic lubricant oils.
  • a preferred example of natural lubricant oil is mineral oil.
  • Other, synthetic lubricant oils including alkylbenzene, polyol ester, polyalkylene glycols, polyvinyl ethers, carbonates and polyalphaolefin may also be used.
  • perfluoropolyether is used together with mineral oil. In another aspect of the invention, perfluoropolyether is used together with synthetic lubricant oils.
  • the amount of perfluoropolyether is less than 50% by weight relative to the mineral oil.
  • the amount of perfluoropolyether is less than 20% by weight relative to the mineral oil. More preferably, the amount of perfluoropolyether is less than 5% by weight relative to the mineral oil. Most preferably, the amount of perfluoropolyether is less than 3 wt. % relative to the mineral oil.
  • the refrigeration or heat transfer fluid composition comprises a mineral oil, perfluoropolyether, and a refrigeration or heat transfer fluid selected from the group consisting of R-407C, R-422A, R-417A, R-404A, R-410A, R-507A, R-508A, R422A, R-417A, and HFC-134a.
  • the refrigeration or heat transfer fluid composition comprises a perfluoropolyether and an unsaturated fluorocarbon such as 1,2,3,3,3-pentafluoro-1-propene, 1,1,3,3,3-pentafluoro-1-propene, 1,1,2,3,3-pentafluoro-1-propene, 1,2,3,3-tetrafluoro-1-propene, 2,3,3,3-tetrafluoro-1-propene, 1,3,3,3-tetrafluoro-1-propene, 1,1,2,3-tetrafluoro-1-propene, 1,1,3,3-tetrafluoro-1-propene, 1,2,3,3-tetrafluoro-1-propene, 1,1,1,2,3,4,4,4-octafluoro-2-butene, 1,1,1,2,4,4,4-heptafluoro-2-butene, or 1,1,1,4,4,4-hexafluoro-2-butene.
  • the present invention further relates to a method of using the refrigeration or heat transfer fluid compositions of the present invention for producing refrigeration or heating, wherein the method comprises producing refrigeration by evaporating said composition in the vicinity of a body to be cooled and thereafter condensing said composition; or producing heat by condensing said composition in the vicinity of the body to be heated and thereafter evaporating said composition.
  • the present invention further relates to a process for transfer of heat from a heat source to a heat sink wherein the compositions of the present invention serve as heat transfer fluids.
  • Said process for heat transfer comprises transferring the compositions of the present invention from a heat source to a heat sink.
  • Heat transfer fluids are utilized to transfer, move or remove heat from one space, location, object or body to a different space, location, object or body by radiation, conduction, or convection.
  • a heat transfer fluid may function as a secondary coolant by providing means of transfer for cooling (or heating) from a remote refrigeration (or heating) system.
  • the heat transfer fluid may remain in a constant state throughout the transfer process (i.e., not evaporate or condense).
  • evaporative cooling processes may utilize heat transfer fluids as well.
  • a heat source may be defined as any space, location, object or body from which it is desirable to transfer, move or remove heat.
  • heat sources may be spaces (open or enclosed) requiring refrigeration or cooling, such as refrigerator or freezer cases in a supermarket, building spaces requiring air-conditioning, or the passenger compartment of an automobile requiring air-conditioning.
  • a heat sink may be defined as any space, location, object or body capable of absorbing heat.
  • a vapor compression refrigeration system is one example of such a heat sink.
  • the present invention further relates to a method of using the perfluoropolyether to maintain or improve the oil return, lubrication, or energy efficiency of the refrigeration, air conditioning and heat transfer system.
  • the method comprises adding an effective amount of perfluoropolyether into the refrigeration or air-conditioning apparatus. This may be done by mixing the perfluoropolyether with the refrigerant or heat transfer fluid compositions of this invention and then introducing the combination into the apparatus. Alternatively, this may be done by directly introducing perfluoropolyether into refrigeration or air-conditioning apparatus containing refrigerant and/or heat transfer fluid to combine in situ with the refrigerant. The resulting composition may be used in the refrigeration or air-conditioning apparatus.
  • the present invention further relates to a method of using the perfluoropolyether to maintain or improve the oil return, lubrication, or energy efficiency by replacing the existing refrigerants or heat transfer fluids without changing the existing lubricants in the refrigeration or air-conditioning apparatus.
  • the method comprises removing the existing refrigerant or heat transfer fluid from the refrigeration or air-conditioning apparatus without flushing out the existing lubricant.
  • Said refrigeration or air-conditioning apparatus is then filled with a pre-mixed composition comprising perfluoropolyether and the refrigerant or heat transfer fluid compositions of this invention.
  • compositions of the present invention may be used in stationary air-conditioning, heat pumps or mobile air-conditioning and refrigeration systems.
  • Stationary air-conditioning and heat pump applications include window, ductless, ducted, packaged terminal, chillers and commercial, including packaged rooftop.
  • Refrigeration applications include domestic or home refrigerators and freezers, ice machines, self-contained coolers and freezers, walk-in coolers and freezers and supermarket systems, and transport refrigeration systems.
  • compositions of the present invention for example, a composition comprising a mineral oil, perfluoropolyether, and a refrigeration or heat transfer fluid selected from the group consisting of R-407C, R-422A, R-417A, R-404A, R-410A, R-507A, R-508A, and HFC-134a
  • Krytox® 157FSH is sufficiently miscible with HFC refrigerants including R-134a, R-125, R-32 such that the Krytox® can be blended with the refrigerant blend and charged to the refrigeration or air conditioning apparatus as a homogeneous liquid.
  • the ZeroZone commercial reach in refrigerator described above was re-fitted with a thermal expansion valve to allow it to operate with the HFC refrigerant R-404A (a blend of 44 wt. % of HFC-125, 52 wt. % of HFC-143a and 4 wt. % of HFC-134a) and Suniso 4GS mineral oil.
  • This refrigerator was operated at an internal box temperature of 38 degrees Fahrenheit while energy consumption was monitored.
  • the test was conducted with the refrigerator in a constant temperature room that was controlled at a constant temperature of 90 degrees Fahrenheit. During a three-hour test period the power consumption of the refrigerator was measured to be at a rate of 22.65 Kilowatt hours per day.
  • the Test set up described in example 6 above was modified by removing the refrigerant charge, and re-charging with a mixture of refrigerant R-404A and Suniso 4GS mineral oil which contained 0.2% by weight, relative to the refrigerant charge, of Krytox® 157 FSH.
  • the test chamber was stabilized again at 90 degrees, and the refrigerator was allowed to operate. Over a three-hour period the internal box temperature was maintained at 37.6 degrees Fahrenheit.
  • the average power use by the refrigerator during this test period was measured to be at a rate of 21.83 Kilowatt hours per day. This was 3.6% less power usage than was measured in Example 6, when no Krytox® was in the refrigerant.
  • Boundary Layer Lubrication tests were run using a FALEX Pin on vee-block test geometry, according to test protocol based on the ASTM 2670-95 Load to Failure test method.
  • a rotating steel pin was squeezed between two standard blocks of aluminum metal.
  • the aluminum blocks were made with vee shaped notches in them, and they were mounted in a bracket such that the vee notches contacted the steel pin.
  • the pin and block assembly was immersed in a pan of lubricant and a motor coupled through a torque meter rotated the pin.
  • the blocks were adjusted to lightly contact the surface of the rotating pin at a low load of 250-pounds pressure for an initial run-in period of five minutes.
  • the force load applied to the blocks was then increased slowly at a steady rate of 200 more pounds each minute by a mechanical tightener that squeezed the rotating pin between the two vee blocks.
  • the load was increased to some predetermined limit, or until a mechanical failure of one of the test pieces occurred.
  • pure Suniso 4GS mineral oil the test failed within the first minute, while the mechanical load on the pin and block assembly was only 250 lb.
  • this test was repeated with a mixture of 0.5% by weight of Krytox® 157 FSL dispersed in the Suniso 4GS mineral oil, the test continued to run for 9 minutes, during which time the mechanical load had increased to a level of 2100 pounds.
  • a split system Carrier heat pump was used to evaluate refrigerant and lubricant performance in air conditioning and heating modes.
  • the system consisted of a condensing unit, Model 38YXA03032, and an evaporator Unit, Model FX4ANF030, and was rated at a nominal cooling capacity of 2 Y2 tons of cooling with R410A.
  • the system was operated inside of a dual chamber psychrometric chamber, with one chamber regulated at outdoor conditions per standard ARI 210/240 Cooling A test conditions, and the other chamber regulated at Cooling A indoor test conditions.
  • This unit was also modified so that the compressor could be changed from the standard R410A rated compressor to a compressor sized for operation with R407C.
  • runs 1,2, and 3 were made using the R-410A compressor. Runs 4, 5, 6, and 7 were made with the R-407C compressor.
  • the copper tubing in the evaporator and condenser coils of this air conditioning system came from the factory with a feature called “internally enhanced heat transfer surfaces”, a feature which is generally known and used throughout the industry.
  • This feature includes fine grooves cut in a spiral or cross hatch pattern on the inside surface of the tube. These grooves cause disruption of the laminar flow layers near the tube surface. The result of this disruption is believed to be improved heat transfer from the evaporating refrigerant within the copper tubes to the tubes themselves and the attached fins that comprise the evaporator unit. Heat transfer to the air flowing through the fins of the evaporator is believed to be thereby improved, with the creation of a more energy efficient air conditioning or heating process.
  • the use of internally enhanced tube surfaces is well known and widely applied within the air conditioning and heat pump industries. Most higher efficiency systems employ enhanced surface tubing in evaporators and condensers.
  • the lubricant 3GS is a commercial naphthenic mineral oil available from Sonneborn, Inc.
  • the mineral oil lubricant is not miscible with HFC refrigerants.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Combustion & Propulsion (AREA)
  • Thermal Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Lubricants (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Paints Or Removers (AREA)
US11/653,125 2006-01-13 2007-01-12 Refrigerant additive compositions containing perfluoropolethers Abandoned US20070187639A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US11/653,125 US20070187639A1 (en) 2006-01-13 2007-01-12 Refrigerant additive compositions containing perfluoropolethers
US11/827,256 US7759532B2 (en) 2006-01-13 2007-07-11 Refrigerant additive compositions containing perfluoropolyethers
US11/827,255 US8188323B2 (en) 2006-01-13 2007-07-11 Refrigerant compositions containing perfluoropolyethers
US12/796,696 US8049046B2 (en) 2006-01-13 2010-06-09 Refrigerant additive compositions containing perfluoropolyethers
US13/241,540 US8426657B2 (en) 2006-01-13 2011-09-23 Refrigerant additive compositions containing perfluoropolyethers
US13/833,524 US8758641B2 (en) 2006-01-13 2013-03-15 Refrigerant additive compositions containing perfluoropolyethers
US14/277,489 US9315709B2 (en) 2006-01-13 2014-05-14 Refrigerant additive compositions containing perfluoropolyethers

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US75873506P 2006-01-13 2006-01-13
US11/653,125 US20070187639A1 (en) 2006-01-13 2007-01-12 Refrigerant additive compositions containing perfluoropolethers

Related Child Applications (3)

Application Number Title Priority Date Filing Date
US11/827,255 Continuation-In-Part US8188323B2 (en) 2006-01-13 2007-07-11 Refrigerant compositions containing perfluoropolyethers
US11/827,255 Continuation US8188323B2 (en) 2006-01-13 2007-07-11 Refrigerant compositions containing perfluoropolyethers
US11/827,256 Continuation-In-Part US7759532B2 (en) 2006-01-13 2007-07-11 Refrigerant additive compositions containing perfluoropolyethers

Publications (1)

Publication Number Publication Date
US20070187639A1 true US20070187639A1 (en) 2007-08-16

Family

ID=37930414

Family Applications (1)

Application Number Title Priority Date Filing Date
US11/653,125 Abandoned US20070187639A1 (en) 2006-01-13 2007-01-12 Refrigerant additive compositions containing perfluoropolethers

Country Status (17)

Country Link
US (1) US20070187639A1 (zh)
EP (2) EP3461872B1 (zh)
JP (1) JP2009523859A (zh)
KR (1) KR20090003165A (zh)
CN (2) CN101370900A (zh)
AU (1) AU2007204857B2 (zh)
BR (1) BRPI0706862A2 (zh)
CA (1) CA2634593C (zh)
DK (2) DK1979432T3 (zh)
ES (2) ES2935258T3 (zh)
MX (1) MX339237B (zh)
NO (1) NO343995B1 (zh)
PL (2) PL3461872T3 (zh)
RU (1) RU2008133202A (zh)
TR (1) TR201902590T4 (zh)
TW (1) TW200738861A (zh)
WO (1) WO2007082046A1 (zh)

Cited By (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009032983A1 (en) 2007-09-06 2009-03-12 E. I. Du Pont De Nemours And Company Azeotropic and azeotrope-like compositions of e-1,1,1,4,4,5,5,5-octafluoro-2-pentene
US20090183856A1 (en) * 2008-01-23 2009-07-23 Bulinski Michael J Heat transfer apparatus and methods including hydrofluorocarbonates
WO2009137658A2 (en) * 2008-05-07 2009-11-12 E. I. Du Pont De Nemours And Company Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
WO2009146122A1 (en) 2008-04-04 2009-12-03 Dow Global Technologies Inc. Refrigerant composition
US20100025619A1 (en) * 2006-07-12 2010-02-04 Solvay Fluor Gmbh Method for heating and cooling using fluoroether compounds, compositions suitable therefore and their use
WO2010034698A1 (en) * 2008-09-26 2010-04-01 Solvay Solexis S.P.A. Method for transferring heat
US20110001080A1 (en) * 2008-03-07 2011-01-06 Arkema Inc. Stable formulated systems with chloro-3,3,3-trifluoropropene
US20110000253A1 (en) * 2008-03-07 2011-01-06 Idemitsu Kosan Co., Ltd. Lubricant composition for refrigerating machine
US20110160113A1 (en) * 2006-02-28 2011-06-30 E. I. Du Pont De Nemours And Company Azeotropic compositions comprising fluorinated compounds for cleaning applications
US20120032106A1 (en) * 2008-04-28 2012-02-09 Honeywell International Inc. Refrigerant compositions having a siloxane solubilizing agent
KR101141510B1 (ko) * 2008-03-07 2012-05-24 알케마 인코포레이티드 클로로-3,3,3-트리플루오로프로펜을 갖는 안정한 배합 시스템
CN103237864A (zh) * 2010-12-03 2013-08-07 阿克马法国公司 包含1,1,1,4,4,4-六氟丁-2-烯和3,3,4,4,4-五氟丁-1-烯的组合物
WO2014172272A1 (en) 2013-04-16 2014-10-23 E. I. Du Pont De Nemours And Company Methods and apparatus using refrigerant compositions comprising refrigerant and lubricant comprising perfluoropolyether and non-fluorinated lubricant
US9145507B2 (en) 2011-07-01 2015-09-29 Arkema France Compositions of 2,4,4,4-tetrafluorobut-1-ene and cis-1,1,1,4,4,4-hexafluorobut-2-ene
WO2015149157A1 (en) * 2014-04-04 2015-10-08 Brasscorp Limited Additive composition for improvement of miscibility of lubricants in air-conditioning and refrigeration systems
US9157018B2 (en) 2010-11-25 2015-10-13 Arkema France Compositions of chloro-trifluoropropene and hexafluorobutene
US9267066B2 (en) 2010-11-25 2016-02-23 Arkema France Refrigerants containing (E)-1,1,1,4,4,4-hexafluorobut-2-ene
US9909045B2 (en) 2012-04-04 2018-03-06 Arkema France Compositions based on 2,3,3,4,4,4-hexafluorobut-1-ene
US20180215979A1 (en) * 2015-07-28 2018-08-02 The Chemours Company Fc, Llc Use of 1,3,3,4,4,4-hexafluoro-1-butene in power cycles
WO2019147363A1 (en) 2018-01-23 2019-08-01 The Chemours Company Fc, Llc Compositions, system and methods for introducing pag lubricant or refrigerant into an air-conditioning or system using lower or low gwp refrigerant or refrigerant blends
WO2019147364A1 (en) 2018-01-23 2019-08-01 The Chemours Company Fc, Llc Compositions, system and methods for introducing poe lubricant into an electric (hev, phev, ev) automotive air-conditioning/heating system or stationary air-conditioning/heating system or stationary refrigeration system using lower or low gwp refrigerant or refrigerant blends
WO2020106930A1 (en) * 2018-11-21 2020-05-28 Honeywell International Inc. Nonflammable refrigerants having low gwp, and systems for and methods of providing refrigeration
WO2020127665A1 (en) 2018-12-20 2020-06-25 Solvay Specialty Polymers Italy S.P.A. Method for exchanging heat with a battery using fluorinated compounds having a low gwp
WO2020127771A1 (en) 2018-12-20 2020-06-25 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using fluorinated compounds having a low gwp
WO2020127666A1 (en) 2018-12-20 2020-06-25 Solvay Specialty Polymers Italy S.P.A. Method of manufacturing semiconductor devices using a heat transfer fluid comprising fluorinated compounds having a low gwp
WO2020187839A1 (en) 2019-03-18 2020-09-24 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using fluorinated compounds having a low gwp
US10883063B2 (en) 2018-01-23 2021-01-05 The Chemours Company Fc, Llc Compositions, system and methods for introducing PAG lubricant or refrigerant into an air-conditioning or system using lower or low GWP refrigerant or refrigerant blends
WO2021008949A1 (en) 2019-07-18 2021-01-21 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using fluorinated compounds having a low gwp
US10913913B2 (en) 2018-01-23 2021-02-09 The Chemours Company Fc, Llc Polyol ester compositions
WO2022043268A1 (en) 2020-08-28 2022-03-03 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using fluorinated vinylethers having a low gwp
WO2024056187A1 (en) 2022-09-16 2024-03-21 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using low gwp fluids
WO2024056188A1 (en) 2022-09-16 2024-03-21 Solvay Specialty Polymers Italy S.P.A. Fluorinated nitro compounds having a low global warming potential

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008027512A2 (en) * 2006-09-01 2008-03-06 E. I. Du Pont De Nemours And Company Functionalized perfluoropolyether stabilizers for fluoroolefins
JP5176624B2 (ja) * 2008-03-18 2013-04-03 ダイキン工業株式会社 冷凍装置
JP2010060262A (ja) * 2008-08-04 2010-03-18 Sanden Corp 冷凍回路用樹脂材料
FR2948679B1 (fr) * 2009-07-28 2011-08-19 Arkema France Procede de transfert de chaleur
WO2011082046A1 (en) 2009-12-30 2011-07-07 3M Innovative Properties Company Copolymers with perfluorpolyether segment and multiple aminooxalylamino groups
CN102712750B (zh) 2009-12-30 2014-06-25 3M创新有限公司 具有乙二酰胺基团的含全氟聚醚化合物
KR101820979B1 (ko) 2009-12-30 2018-01-22 쓰리엠 이노베이티브 프로퍼티즈 컴파니 폴리다이오르가노실록산 폴리옥사미드 공중합체의 제조 방법
WO2011082063A1 (en) 2009-12-30 2011-07-07 3M Innovative Properties Company Copolymers with perfluorpolyether segment and polydiorganosiloxane segment
EP2386583A1 (en) 2010-05-07 2011-11-16 Borealis AG Process for the preparation of a solid metallocene catalyst system and its use in polymerisation of olefins
EP2385073A1 (en) 2010-05-07 2011-11-09 Borealis AG Process for the preparation of a solid metallocene catalyst system and its use in polymerisation of olefins
FR2964976B1 (fr) * 2010-09-20 2012-08-24 Arkema France Composition a base de 1,3,3,3-tetrafluoropropene
CN103547552B (zh) * 2011-05-19 2017-02-08 阿科玛股份有限公司 氯三氟丙烯的不可燃氯组合物
FR2988729B1 (fr) * 2012-03-29 2014-03-14 Arkema France Compositions de 2,4,4,4-tetrafluorobut-1-ene et de 1-methoxyheptafluoropropane
CN103105085A (zh) * 2013-02-01 2013-05-15 北京工业大学 一种汽车尾气余热回收熔盐传热蓄热换热器
CN103509520A (zh) * 2013-08-01 2014-01-15 广东美芝制冷设备有限公司 组合物以及采用该组合物的压缩机和制冷设备
GB201418709D0 (en) 2014-10-21 2014-12-03 Mexichem Fluor Sa De Cv Compound
JP2016160234A (ja) * 2015-03-03 2016-09-05 旭硝子株式会社 ヘキサフルオロブテンの製造方法
JP6749768B2 (ja) * 2016-02-10 2020-09-02 三菱重工サーマルシステムズ株式会社 熱源機およびその運転方法
WO2019208382A1 (ja) * 2018-04-25 2019-10-31 ダイキン工業株式会社 冷媒を含有する組成物、熱移動媒体及び熱サイクルシステム
CN108841360B (zh) * 2018-06-22 2020-11-03 东阳市巍华制冷材料有限公司 一种含全氟甲基乙烯基醚的组合物制冷剂
CN109652235B (zh) * 2018-09-29 2020-11-13 天津市长芦化工新材料有限公司 共沸组合物及其应用
US11932589B2 (en) * 2019-02-19 2024-03-19 3M Innovative Properties Company Hydrofluoroolefins and methods of using same
CN111792985B (zh) * 2019-07-17 2022-10-14 泉州宇极新材料科技有限公司 一种含氟传热流体及其制备方法和应用
CN111793475B (zh) * 2019-07-17 2021-11-02 泉州宇极新材料科技有限公司 一种热传递装置及方法
CN110684509B (zh) * 2019-09-12 2020-09-25 珠海格力电器股份有限公司 一种环保混合制冷剂及换热系统
CN113621352B (zh) * 2021-06-25 2023-07-07 浙江巨化技术中心有限公司 一种组合物、液冷剂及其应用以及浸没冷却系统

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5221494A (en) * 1989-06-05 1993-06-22 Asahi Kasei Kogyo Kabushiki Kaisha Refrigerant composition comprising tetrafluoroethane refrigerant and lubricant having miscibility therewith at low temperature
US6221273B1 (en) * 1997-07-11 2001-04-24 Ausimont S.P.A. Refrigerating compositions based on hexafluoropropane, fluoroethers and hydrocarbons
US20030040445A1 (en) * 2000-01-31 2003-02-27 Imperial Chemical Industries Plc Refrigerant lubrificant composition comprising a foam-inducing additive
US20040013610A1 (en) * 2000-11-08 2004-01-22 Pierre Dournel Solvent compositions
US6982173B2 (en) * 2001-06-26 2006-01-03 Solvay Solexis, S.P.A. PFPEs having at least an alkylether end group and respective preparation process

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62146996A (ja) * 1985-12-20 1987-06-30 Nishi Nippon Tsusho Kk 冷凍機油組成物
JPS62288692A (ja) * 1986-06-06 1987-12-15 Hitachi Ltd フロン圧縮機用潤滑油
JP2771539B2 (ja) * 1987-11-02 1998-07-02 出光興産株式会社 フロン冷媒用潤滑油
JPH037798A (ja) * 1989-06-05 1991-01-14 Asahi Chem Ind Co Ltd 冷凍機用潤滑油
JPH04288452A (ja) * 1991-03-15 1992-10-13 Daikin Ind Ltd 冷凍機の運転方法
JP3612805B2 (ja) * 1995-07-18 2005-01-19 ダイキン工業株式会社 冷凍機
EP1306417B1 (en) * 2001-10-23 2012-08-01 Solvay Specialty Polymers Italy S.p.A. Use of fluorinated liquids for the heat exchange or as working fluids in the presence of ionizing radiations and/or irradiation with neutrons
ITMI20020012A1 (it) * 2002-01-08 2003-07-08 Ausimont Spa Uso di liquidi fluorurati
US7279451B2 (en) * 2002-10-25 2007-10-09 Honeywell International Inc. Compositions containing fluorine substituted olefins
US7655610B2 (en) * 2004-04-29 2010-02-02 Honeywell International Inc. Blowing agent compositions comprising fluorinated olefins and carbon dioxide
US7524805B2 (en) * 2004-04-29 2009-04-28 Honeywell International Inc. Azeotrope-like compositions of tetrafluoropropene and hydrofluorocarbons
WO2005049760A1 (en) * 2003-11-13 2005-06-02 E.I. Dupont De Nemours And Company Compositions and methods for reducing fire hazard of flammable refrigerants

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5221494A (en) * 1989-06-05 1993-06-22 Asahi Kasei Kogyo Kabushiki Kaisha Refrigerant composition comprising tetrafluoroethane refrigerant and lubricant having miscibility therewith at low temperature
US6221273B1 (en) * 1997-07-11 2001-04-24 Ausimont S.P.A. Refrigerating compositions based on hexafluoropropane, fluoroethers and hydrocarbons
US20030040445A1 (en) * 2000-01-31 2003-02-27 Imperial Chemical Industries Plc Refrigerant lubrificant composition comprising a foam-inducing additive
US20040013610A1 (en) * 2000-11-08 2004-01-22 Pierre Dournel Solvent compositions
US6982173B2 (en) * 2001-06-26 2006-01-03 Solvay Solexis, S.P.A. PFPEs having at least an alkylether end group and respective preparation process

Cited By (70)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110160113A1 (en) * 2006-02-28 2011-06-30 E. I. Du Pont De Nemours And Company Azeotropic compositions comprising fluorinated compounds for cleaning applications
US8044010B2 (en) * 2006-02-28 2011-10-25 E. I. Du Pont De Nemours And Company Azeotropic compositions comprising fluorinated compounds for cleaning applications
US20100025619A1 (en) * 2006-07-12 2010-02-04 Solvay Fluor Gmbh Method for heating and cooling using fluoroether compounds, compositions suitable therefore and their use
WO2009032983A1 (en) 2007-09-06 2009-03-12 E. I. Du Pont De Nemours And Company Azeotropic and azeotrope-like compositions of e-1,1,1,4,4,5,5,5-octafluoro-2-pentene
AU2008296223B2 (en) * 2007-09-06 2013-07-04 E. I. Du Pont De Nemours And Company Azeotropic and azeotrope-like compositions of E-1,1,1,4,4,5,5,5-Octafluoro-2-pentene
US20090183856A1 (en) * 2008-01-23 2009-07-23 Bulinski Michael J Heat transfer apparatus and methods including hydrofluorocarbonates
US8003004B2 (en) 2008-01-23 2011-08-23 3M Innovative Properties Company Heat transfer apparatus and methods including hydrofluorocarbonates
KR101141510B1 (ko) * 2008-03-07 2012-05-24 알케마 인코포레이티드 클로로-3,3,3-트리플루오로프로펜을 갖는 안정한 배합 시스템
US20110001080A1 (en) * 2008-03-07 2011-01-06 Arkema Inc. Stable formulated systems with chloro-3,3,3-trifluoropropene
US20110000253A1 (en) * 2008-03-07 2011-01-06 Idemitsu Kosan Co., Ltd. Lubricant composition for refrigerating machine
US10072192B2 (en) 2008-03-07 2018-09-11 Arkema Inc. Stable formulated systems with chloro-3,3,3-trifluoropropene
US9254468B2 (en) 2008-03-07 2016-02-09 Arkema Inc. Stable formulated systems with chloro-3,3,3-trifluoropropene
US8673169B2 (en) * 2008-03-07 2014-03-18 Idemitsu Kosan Co., Ltd. Lubricant composition for refrigerating machine
US8003003B2 (en) 2008-04-04 2011-08-23 Dow Global Technologies Llc Refrigerant composition
US20090302264A1 (en) * 2008-04-04 2009-12-10 Dow Global Technologies Inc. Refrigerant composition
US8246852B2 (en) 2008-04-04 2012-08-21 Dow Global Technologies Llc Refrigerant composition
WO2009146122A1 (en) 2008-04-04 2009-12-03 Dow Global Technologies Inc. Refrigerant composition
US8765006B2 (en) * 2008-04-28 2014-07-01 Honeywell International Inc. Refrigerant compositions having a siloxane solubilizing agent
US20120032106A1 (en) * 2008-04-28 2012-02-09 Honeywell International Inc. Refrigerant compositions having a siloxane solubilizing agent
EP4056661A1 (en) * 2008-05-07 2022-09-14 The Chemours Company FC, LLC Compositions comprising 2,3,3,3-tetrafluoropropene
US11512239B2 (en) 2008-05-07 2022-11-29 The Chemours Company Fc, Llc Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
US9486657B2 (en) 2008-05-07 2016-11-08 The Chemours Company Fc, Llc Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
WO2009137658A3 (en) * 2008-05-07 2009-12-30 E. I. Du Pont De Nemours And Company Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
US11312890B2 (en) 2008-05-07 2022-04-26 The Chemours Company Fc, Llc Compositions comprising 2,3-dichloro-1,1,1 -trifluoropropane, 2-chloro-1,1,1 -trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
US8877086B2 (en) 2008-05-07 2014-11-04 E I Du Pont De Nemours And Company Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
US11001738B2 (en) 2008-05-07 2021-05-11 The Chemours Company Fc, Llc Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
US10584270B2 (en) 2008-05-07 2020-03-10 The Chemours Company Fc, Llc Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
US10214669B2 (en) 2008-05-07 2019-02-26 The Chemours Company Fc, Llc Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
WO2009137658A2 (en) * 2008-05-07 2009-11-12 E. I. Du Pont De Nemours And Company Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene
US8999192B2 (en) 2008-09-26 2015-04-07 Solvay Specialty Polymers Italy S.P.A. Method for transferring heat
US20110175016A1 (en) * 2008-09-26 2011-07-21 Solvay Solexis S.P.A. Method for transferring heat
WO2010034698A1 (en) * 2008-09-26 2010-04-01 Solvay Solexis S.P.A. Method for transferring heat
US9528039B2 (en) 2010-11-25 2016-12-27 Arkema France Refrigerants containing (E)-1,1,1,4,4,4-hexafluorobut-2-ene
US9157018B2 (en) 2010-11-25 2015-10-13 Arkema France Compositions of chloro-trifluoropropene and hexafluorobutene
US10407603B2 (en) 2010-11-25 2019-09-10 Arkema France Compositions of chloro-trifluoropropene and hexafluorobutene
US9528038B2 (en) 2010-11-25 2016-12-27 Arkema France Compositions of chloro-trifluoropropene and hexafluorobutene
US9267066B2 (en) 2010-11-25 2016-02-23 Arkema France Refrigerants containing (E)-1,1,1,4,4,4-hexafluorobut-2-ene
US9982178B2 (en) 2010-11-25 2018-05-29 Arkema France Compositions of chloro-trifluoropropene and hexafluorobutene
US10150901B2 (en) * 2010-12-03 2018-12-11 Arkema France Compositions containing 1,1,1,4,4,4-hexafluorobut-2-ene and 3,3,4,4,4-petrafluorobut-1-ene
CN103237864A (zh) * 2010-12-03 2013-08-07 阿克马法国公司 包含1,1,1,4,4,4-六氟丁-2-烯和3,3,4,4,4-五氟丁-1-烯的组合物
US20130247602A1 (en) * 2010-12-03 2013-09-26 Arkema France Compositions containing 1,1,1,4,4,4-hexafluorobut-2-ene and 3,3,4,4,4-petrafluorobut-1-ene
US9145507B2 (en) 2011-07-01 2015-09-29 Arkema France Compositions of 2,4,4,4-tetrafluorobut-1-ene and cis-1,1,1,4,4,4-hexafluorobut-2-ene
US9359541B2 (en) 2011-07-01 2016-06-07 Arkema France Compositions of 2,4,4,4-tetrafluorobut-1-ene and cis-1,1,1,4,4,4-hexafluorobut-2-ene
US9909045B2 (en) 2012-04-04 2018-03-06 Arkema France Compositions based on 2,3,3,4,4,4-hexafluorobut-1-ene
CN105378023A (zh) * 2013-04-16 2016-03-02 得凯莫斯公司弗罗里达有限公司 使用包含制冷剂及含全氟聚醚和非氟化润滑剂的制冷剂组合物的方法和设备
WO2014172272A1 (en) 2013-04-16 2014-10-23 E. I. Du Pont De Nemours And Company Methods and apparatus using refrigerant compositions comprising refrigerant and lubricant comprising perfluoropolyether and non-fluorinated lubricant
US10514190B2 (en) 2014-04-04 2019-12-24 Alltemp Products Company Limited Additive composition for improvement of miscibility of lubricants in air-conditioning and refrigeration systems
WO2015149157A1 (en) * 2014-04-04 2015-10-08 Brasscorp Limited Additive composition for improvement of miscibility of lubricants in air-conditioning and refrigeration systems
US11085678B2 (en) 2014-04-04 2021-08-10 Alltemp Products Company Limited Additive composition for improvement of miscibility of lubricants in air-conditioning and refrigeration systems
US20180215979A1 (en) * 2015-07-28 2018-08-02 The Chemours Company Fc, Llc Use of 1,3,3,4,4,4-hexafluoro-1-butene in power cycles
US11427777B2 (en) 2018-01-23 2022-08-30 The Chemours Company Fc, Llc Compositions, system and methods for introducing PAG lubricant or refrigerant into an air-conditioning or system using lower or low GWP refrigerant or refrigerant blends
US11453834B2 (en) 2018-01-23 2022-09-27 The Chemours Company Fc, Llc Compositions, system and methods for introducing POE lubricant into an air-conditioning or a refrigeration system
US10883063B2 (en) 2018-01-23 2021-01-05 The Chemours Company Fc, Llc Compositions, system and methods for introducing PAG lubricant or refrigerant into an air-conditioning or system using lower or low GWP refrigerant or refrigerant blends
EP4306878A2 (en) 2018-01-23 2024-01-17 The Chemours Company FC, LLC Compositions, system and methods for introducing poe lubricant into an electric (hev, phev, ev) automotive air-conditioning/heating system or stationary air-conditioning/heating system or stationary refrigeration system using lower or low gwp refrigerant
US10913913B2 (en) 2018-01-23 2021-02-09 The Chemours Company Fc, Llc Polyol ester compositions
US11802253B2 (en) 2018-01-23 2023-10-31 The Chemours Company Fc, Llc Compositions, system and methods for introducing PAG lubricant or refrigerant into an air-conditioning or system using lower or low GWP refrigerant or refrigerant blends
EP4194532A1 (en) 2018-01-23 2023-06-14 The Chemours Company FC, LLC Compositions, system and methods for introducing poe lubricant into an electric (hev, phev, ev) automotive air-conditioning/heating system or stationary air-conditioning/heating system or stationary refrigeration system using lower or low gwp refrigerant blends
WO2019147363A1 (en) 2018-01-23 2019-08-01 The Chemours Company Fc, Llc Compositions, system and methods for introducing pag lubricant or refrigerant into an air-conditioning or system using lower or low gwp refrigerant or refrigerant blends
EP3967737A1 (en) 2018-01-23 2022-03-16 The Chemours Company FC, LLC Compositions, system and methods for introducing pag lubricant or refrigerant into an air-conditioning or system using lower or low gwp refrigerant or refrigerant blends
EP4067454A1 (en) 2018-01-23 2022-10-05 The Chemours Company FC, LLC Compositions, system and methods for introducing pag lubricant or refrigerant into an air conditioning or system using lower or low gwp refrigerant or refrigerant blends
WO2019147364A1 (en) 2018-01-23 2019-08-01 The Chemours Company Fc, Llc Compositions, system and methods for introducing poe lubricant into an electric (hev, phev, ev) automotive air-conditioning/heating system or stationary air-conditioning/heating system or stationary refrigeration system using lower or low gwp refrigerant or refrigerant blends
WO2020106930A1 (en) * 2018-11-21 2020-05-28 Honeywell International Inc. Nonflammable refrigerants having low gwp, and systems for and methods of providing refrigeration
WO2020127666A1 (en) 2018-12-20 2020-06-25 Solvay Specialty Polymers Italy S.P.A. Method of manufacturing semiconductor devices using a heat transfer fluid comprising fluorinated compounds having a low gwp
WO2020127665A1 (en) 2018-12-20 2020-06-25 Solvay Specialty Polymers Italy S.P.A. Method for exchanging heat with a battery using fluorinated compounds having a low gwp
WO2020127771A1 (en) 2018-12-20 2020-06-25 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using fluorinated compounds having a low gwp
WO2020187839A1 (en) 2019-03-18 2020-09-24 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using fluorinated compounds having a low gwp
WO2021008949A1 (en) 2019-07-18 2021-01-21 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using fluorinated compounds having a low gwp
WO2022043268A1 (en) 2020-08-28 2022-03-03 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using fluorinated vinylethers having a low gwp
WO2024056187A1 (en) 2022-09-16 2024-03-21 Solvay Specialty Polymers Italy S.P.A. Heat exchange method using low gwp fluids
WO2024056188A1 (en) 2022-09-16 2024-03-21 Solvay Specialty Polymers Italy S.P.A. Fluorinated nitro compounds having a low global warming potential

Also Published As

Publication number Publication date
RU2008133202A (ru) 2010-02-20
CA2634593A1 (en) 2007-07-19
EP1979432A1 (en) 2008-10-15
EP3461872A1 (en) 2019-04-03
TR201902590T4 (tr) 2019-03-21
ES2712097T3 (es) 2019-05-09
BRPI0706862A2 (pt) 2011-04-12
NO343995B1 (no) 2019-08-12
DK3461872T3 (da) 2023-01-30
AU2007204857B2 (en) 2012-12-13
NO20083402L (no) 2008-10-03
JP2009523859A (ja) 2009-06-25
CA2634593C (en) 2016-12-20
DK1979432T3 (en) 2019-04-01
MX339237B (es) 2016-05-18
TW200738861A (en) 2007-10-16
PL1979432T3 (pl) 2019-05-31
WO2007082046A1 (en) 2007-07-19
CN103834365A (zh) 2014-06-04
PL3461872T3 (pl) 2023-02-06
ES2935258T3 (es) 2023-03-03
EP3461872B1 (en) 2022-11-09
KR20090003165A (ko) 2009-01-09
CN101370900A (zh) 2009-02-18
EP1979432B1 (en) 2018-12-05
AU2007204857A1 (en) 2007-07-19
CN103834365B (zh) 2017-01-11

Similar Documents

Publication Publication Date Title
EP1979432B1 (en) Refrigerant additive compositions containing perfluoropolyethers
US9315709B2 (en) Refrigerant additive compositions containing perfluoropolyethers
US8188323B2 (en) Refrigerant compositions containing perfluoropolyethers
US20160068731A1 (en) Methods and apparatus using refrigerant compositions comprising refrigerant and lubricant comprising perfluoropolyether and non-fluorinated lubricant
US20120032106A1 (en) Refrigerant compositions having a siloxane solubilizing agent
TWI640617B (zh) 包含氟化烯烴/氟化飽和烴摻和物及聚醇酯之工作流體
EP3313965B1 (en) Working fluids comprising fluorinated olefins and polyol esters
AU2013201452B2 (en) Refrigerant additive compositions containing perfluoropolyethers
MX2008008927A (en) Refrigerant additive compositions containing perfluoropolyethers
JP3347614B2 (ja) 冷凍機油組成物及び該組成物を用いた潤滑方法
BRPI0706862B1 (pt) Compositions, method of cooling production, method of producing heat, process of heat transfer, process of replacement of refrigerant or heat transfer fluid, refrigeration system, air conditioning appliances and heating pumps with transfer surfaces of heat

Legal Events

Date Code Title Description
AS Assignment

Owner name: E. I. DU PONT DE NEMOURS AND COMPANY, DELAWARE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LECK, THOMAS J.;BELL, GREGORY A.;SATURNO, THOMAS FRANK;REEL/FRAME:019259/0969;SIGNING DATES FROM 20070409 TO 20070418

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION